Fluphenazine decanoate
目录号: PL09224 纯度: ≥98.0%
CAS No. :5002-47-1
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PL09224-10mg 10mg ¥507.50 请登录
PL09224-50mg 50mg ¥2152.50 请登录
PL09224-100mg 100mg ¥3815.00 请登录
PL09224-200mg 200mg 询价 询价
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PL09224-10mM*1mLinDMSO 10mM*1mLinDMSO ¥1334.00 请登录
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中文名称
Fluphenazine decanoate
中文别名
癸氟奋乃静;4-[3-[2-(三氟甲基)-10H-吩噻嗪-10-基]丙基]-1-哌嗪乙醇癸酸酯;氟奋乃静癸;氟奋乃静癸酸酯;癸酸氟奋乃静;保利坤
英文名称
Fluphenazine decanoate
英文别名
Fluphenazine decanoate;Fluphenazine O-decanoate;2-[4-[3-[2-(trifluoromethyl)phenothiazin-10-yl]propyl]piperazin-1-yl]ethyl decanoate;FLUPHENAZINE DECANOATE, EP STANDARD;1-decanoyloxy-2-{4-[3-(2-trifluoromethyl-phenothiazin-10-yl)-propyl]-piperazin-1-yl}-ethane;Dapotum D;EP4;Flufenazine decanoate;Fluorophenazine decanoate;Fluphenaline decanoate;Fluphenazindecanat;Fluphenazindecanoat;FLUPHENAZINE DECANOATE,BP2003;Fluphenazine depot;Modecate;Moditen depot;Moditen-depo;USP27
Cas No.
5002-47-1
分子式
C32H44F3N3O2S
分子量
591.77
包装储存
Pure form -20°C 3 years;4°C 2 years
产品详情
Fluphenazine decanoate 是一种多巴胺 D2 受体抑制剂和吩噻嗪类精神安定剂 (neuroleptic)。Fluphenazine decanoate可用于精神分裂症的研究。
生物活性
Fluphenazine decanoate is a dopamine D 2 receptor inhibitor, is a long-acting phenothiazine neuroleptic. Fluphenazine can be used for schizophrenia research.
性状
Oil
IC50 & Target[1][2]
D2 Receptor
体外研究(In Vitro)
Fluphenazine decanoate shows activity against T. gondii in human fibroblast cell cultures with an IC50 value of 1.7 mM.
has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
Fluphenazine decanoate (0.22 mg/kg and followed by 0.33 mg/kg; i.m.; 8 times every 3 weeks), as an antipsychotic, increases sensitivity to dopamine on monkey model following extended treatment.
Fluphenazine decanoate (25 mg/kg; i.m.; 6 times every 3 weeks; 24 weeks) induces mouth movements in the rat, serves as a pharmacological model of human tardive dyskinesia.
Fluphenazine decanoate (1, 2, 3 mg/kg/d; s.c.; 60 d) shows antifertility effects and induces hyperprolactinemia concomitant with gonadotropin suppression in adult male rat.
has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Pure form -20°C 3 years;4°C 2 years
ClinicalTrial
参考文献
[1]. Goodwin DG, et al. Evaluation of five antischizophrenic agents against Toxoplasma gondii in human cell cultures. J Parasitol. 2011 Feb;97(1):148-51.
[2]. Lifshitz K, et al. Effects of dopamine agonists on Cebus apella monkeys with previous long-term exposure to fluphenazine. Biol Psychiatry. 1997 Mar 15;41(6):657-67.
溶解度数据
In Vitro: DMSO : 125 mg/mL (211.23 mM; Need ultrasonic)Ethanol : 50 mg/mL (84.49 mM; Need ultrasonic)配制储备液
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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